| Year |
Citation |
Score |
| 2023 |
McKinzie CJ, Gower WA, Hagood JS, Vece TJ. Use of pirfenidone in pediatric patients with interstitial lung disease and pulmonary fibrosis. Pediatric Pulmonology. PMID 37161910 DOI: 10.1002/ppul.26465 |
0.305 |
|
| 2022 |
Popler J, Vece TJ, Liptzin DR, Gower WA. Pediatric pulmonology 2021 year in review: Rare and diffuse lung disease. Pediatric Pulmonology. PMID 36426677 DOI: 10.1002/ppul.26227 |
0.369 |
|
| 2022 |
Gutierrez MJ, Nino G, Sun D, Restrepo-Gualteros S, Sadreameli SC, Fiorino EK, Wu E, Vece T, Hagood JS, Maglione PJ, Kurland G, Koumbourlis A, Sullivan KE. The lung in inborn errors of immunity: From clinical disease patterns to molecular pathogenesis. The Journal of Allergy and Clinical Immunology. PMID 36244852 DOI: 10.1016/j.jaci.2022.08.024 |
0.391 |
|
| 2022 |
Vece TJ, Gower WA, Davis SD, Austin A, McKinzie CJ, Hatch JE, Davis M, Hagood JS. Building a pediatric rare lung disease program: It takes a community of villages. Pediatric Pulmonology. PMID 35932221 DOI: 10.1002/ppul.26083 |
0.305 |
|
| 2021 |
Vece TJ, Popler J, Gower WA. Pediatric pulmonology 2020 year in review: Rare and diffuse lung disease. Pediatric Pulmonology. PMID 34964566 DOI: 10.1002/ppul.25807 |
0.369 |
|
| 2021 |
Bradford L, Ross MK, Minso J, Cernelc-Kohan M, Shayan K, Wong SS, Li X, Rivier L, Jegga AG, Deutsch GH, Vece TJ, Loughlin CE, Gower WA, Hurley C, Furman W, et al. Interstitial Lung Disease in Children with Rubinstein-Taybi Syndrome. Pediatric Pulmonology. PMID 34585851 DOI: 10.1002/ppul.25709 |
0.39 |
|
| 2021 |
Gower WA, Vece TJ. Pediatric pulmonology 2019 year in review: rare and diffuse lung disease. Pediatric Pulmonology. PMID 33559960 DOI: 10.1002/ppul.25297 |
0.392 |
|
| 2019 |
Vece TJ, Esther CR. Identifying Biomarkers in Pediatric Rare Lung Disease: chILD Grows Up. American Journal of Respiratory and Critical Care Medicine. PMID 31454262 DOI: 10.1164/rccm.201908-1594ED |
0.33 |
|
| 2016 |
Stray-Pedersen A, Sorte HS, Samarakoon P, Gambin T, Chinn IK, Coban Akdemir ZH, Erichsen HC, Forbes LR, Gu S, Yuan B, Jhangiani SN, Muzny DM, Rødningen OK, Sheng Y, Nicholas SK, ... ... Vece TJ, et al. Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders. The Journal of Allergy and Clinical Immunology. PMID 27577878 DOI: 10.1016/J.Jaci.2016.05.042 |
0.355 |
|
| 2016 |
Singla S, Canter DL, Vece TJ, Muscal E, DeGuzman M. Diffuse Alveolar Hemorrhage as a Manifestation of Childhood-Onset Systemic Lupus Erythematosus. Hospital Pediatrics. PMID 27390368 DOI: 10.1542/Hpeds.2015-0281 |
0.339 |
|
| 2016 |
Vece TJ, Watkin LB, Nicholas SK, Canter D, Braun MC, Guillerman RP, Eldin KW, Bertolet G, McKinley SD, de Guzman M, Forbes LR, Chinn I, Orange JS. Copa Syndrome: a Novel Autosomal Dominant Immune Dysregulatory Disease. Journal of Clinical Immunology. PMID 27048656 DOI: 10.1007/S10875-016-0271-8 |
0.372 |
|
| 2015 |
Montella S, Vece TJ, Langston C, Carrera P, Nogee LM, Hamvas A, Manna A, Cervasio M, Santamaria F. Erratum to: A disorder of surfactant metabolism without identified genetic mutations. Italian Journal of Pediatrics. 41: 98. PMID 26672746 DOI: 10.1186/S13052-015-0205-8 |
0.302 |
|
| 2015 |
Montella S, Vece TJ, Langston C, Carrera P, Nogee LM, Hamvas A, Manna A, Cervasio M, Santamaria F. A disorder of surfactant metabolism without identified genetic mutations. Italian Journal of Pediatrics. 41: 93. PMID 26606984 DOI: 10.1186/S13052-015-0198-3 |
0.438 |
|
| 2015 |
Vece TJ, Young LR. Update on Diffuse Lung Disease in Children. Chest. PMID 26502226 DOI: 10.1378/Chest.15-1986 |
0.451 |
|
| 2015 |
Watkin LB, Jessen B, Wiszniewski W, Vece TJ, Jan M, Sha Y, Thamsen M, Santos-Cortez RL, Lee K, Gambin T, Forbes LR, Law CS, Stray-Pedersen A, Cheng MH, Mace EM, et al. COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis. Nature Genetics. 47: 654-60. PMID 25894502 DOI: 10.1038/Ng.3279 |
0.354 |
|
| 2013 |
Chokshi NY, Seth N, Afanador M, Seeborg F, Reid B, Vece T, Orange J, Hanson IC. Chronic Non-Iatrogenic Chylous Loss Syndromes in Children: Are They Primary Immune Deficiencies? Journal of Allergy and Clinical Immunology. 131: AB69. DOI: 10.1016/J.Jaci.2012.12.911 |
0.311 |
|
| 2012 |
Vece TJ, Schecter MG, Gatti RA, Tunuguntla R, Garcia CK, Langston C, Dishop MK, Moore RH, Fan LL. Rapid and progressive pulmonary fibrosis in 2 families with DNA repair deficiencies of undetermined etiology. The Journal of Pediatrics. 160: 700-702.e3. PMID 22240110 DOI: 10.1016/J.Jpeds.2011.12.001 |
0.375 |
|
| 2011 |
Vece TJ, Fan LL. Diagnosis and management of diffuse lung disease in children. Paediatric Respiratory Reviews. 12: 238-42. PMID 22018037 DOI: 10.1016/J.Prrv.2011.04.001 |
0.438 |
|
| 2010 |
Vece TJ, Fan LL. Interstitial Lung Disease in Children Older Than 2 Years. Pediatric Allergy, Immunology, and Pulmonology. 23: 33-41. PMID 22332030 DOI: 10.1089/Ped.2010.0008 |
0.446 |
|
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